H NMR characterization of chitin tetrasaccharide in binary HO:DMSO solution: Evidence for anomeric end-effect propagation.

Kecheng Li, Andrew R Green, Meredith M Dinges, Cynthia K Larive

Journal: International journal of biological macromolecules 2019;129():744-749

PMID: 30771389

Abstract

Chitin oligosaccharides, composed of homogeneous β(1 → 4)-linked N-acetyl-D-glucosamine (GlcNAc) sequences, is a well-known elicitor of plant immune defense, and also occur as structural elements of chitosan and nodulation (Nod) factor. Detailed microstructure characterization is required for understanding the function mode of these bioactive molecules. Herein, experimental conditions for detection and elucidation of the H NMR resonances of amide groups in chitin oligosaccharides are presented. The binary mixture of 70% HO: 30% DMSO‑d was found to be the optimal solvent for amide proton measurements in homogeneous GlcNAc sequences, facilitating differentiation of the local chemical microenvironments of all four amide groups of the chitin tetrasaccharide. Experimental evidence that anomeric end-effect triggers amide proton resonance differentiation at the adjacent residue has potential to provide important insights into the solution structure of chitin and other amino sugars containing GlcNAc sequences.

Copyright © 2019 Elsevier B.V. All rights reserved.

Address: Department of Chemistry, University of California - Riverside, Riverside, CA 92521, United States; Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China; Laboratory for Marine Drugs and Bioproducts of Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, China; Center for Ocean Mega-Science, Chinese Academy of Sciences, Qingdao 266071, China. Electronic address: [email protected].; Department of Chemistry, University of California - Riverside, Riverside, CA 92521, United States.; Department of Chemistry, University of California - Riverside, Riverside, CA 92521, United States. Electronic address: [email protected].

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